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. 2011 Jan 1;22(1):153–164. doi: 10.1091/mbc.E10-08-0732

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© 2011 Helmstaedt et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0).

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FIGURE 6: — CandA-C, but not CandA-N, interacts with deneddylated cullin in vivo. (A) Bimolecular fluorescence complementation (BiFC) of CandA-C with wild-type (CulA; AGB556) or deneddylated (CulA*; AGB557) CulA in the presence of intact untagged CandA-N. (B) Same as (A), but in strains that lack CandA-N (CulA: AGB559 and CulA*: AGB560). (C) BiFC with CandA-N-C fusion and both CulA variants in candA double-deletion background (AGB561, AGB562). (D) BiFC using both CulA variants in combination with nuclear CandA-N (AGB570) and in the absence CandA-C (AGB568). (E) Same as (D), but in strains expressing candA-C (CulA: AGB569 and CulA*: AGB567). Bar, 10 μm. Right-hand schemes summarize interactions.